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1 old nanoparticles followed by imaging with a scanning electron microscope.
2 ith a "nanostressing stage" located within a scanning electron microscope.
3 zing a standardized segment of aorta using a scanning electron microscope.
4 al endothelial structure was examined with a scanning electron microscope.
5 real-time image acquisition in a single-beam scanning electron microscope.
6 orescence microscope (FM) on an existing FIB scanning electron microscope.
7 rent PVA concentrations was observed using a Scanning electron microscope.
8 ic strains during in situ tensile tests in a scanning electron microscope.
9 eestanding membrane of 2D materials inside a scanning electron microscope.
10 paper with immobilized DNA was done using a scanning electron microscope.
11 graphene using a nanomechanical device in a scanning electron microscope.
12 re of kiwifruits slices was examined using a Scanning Electron Microscope.
13 energy-dispersive spectrometer attached to a scanning electron microscope.
14 disk microelectrode arrays was inspected by scanning electron microscope.
15 zed by ATR-FTIR spectrometer, goniometer and scanning electron microscope.
16 and confirmed by using X-ray diffraction and Scanning Electron Microscopes.
17 scopolamine and atropine in the quids, while scanning electron microscope analysis confirms most to b
19 polynuclear sulfur anions as confirmed from scanning electron microscope and energy dispersive X-ray
21 uct nanomechanical experiments in an in situ scanning electron microscope and show that micrometer-si
22 ray Diffraction, Thermogravimetric Analysis, Scanning Electron Microscope and Transmission Electron M
25 or EDS) is a technique often implemented on scanning electron microscopes and a regularly used metho
27 sis, through energy spectrometry utilizing a scanning electron microscope, and by fluorescent microsc
28 ed spectroscopy, thermogravimetric analysis, scanning electron microscope, and energy-dispersive X-ra
29 as characterized by Atomic force microscopy, Scanning electron microscope, and Raman spectroscopy.
30 ons of perfused small vessels were (mean +/- scanning electron microscope) BD rats (40% +/- 6%), sham
31 ble optical cathodoluminescence emitted in a scanning electron microscope by nanoparticles with contr
32 ion of the MAE extracted algal biomass using Scanning electron microscope confirmed the effective cel
34 es using in situ laser illumination inside a scanning electron microscope, coupled with secondary ele
35 ing of the nanobiosensor e.g. field emission scanning electron microscope, cyclic voltammetry and ele
36 hemistry (IHC) staining for collagen IV, and scanning electron microscope demonstrated that the under
37 ted by charge carrier mobility measurements, scanning electron microscope, electron diffraction study
38 smission Electron Microscope, Field Emission Scanning Electron Microscope, Energy Dispersive Analysis
39 essful combination of Raman spectroscopy and scanning electron microscope-energy dispersive X-rays th
40 t in the new resin blocks were examined in a scanning electron microscope equipped for SBF SEM and se
42 s performed within a single focused ion beam scanning electron microscope equipped with an in-house d
47 lues is discussed in light of the results of scanning electron microscope examination of the soil sam
49 sing X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM) and field emission
50 membrane are observed by both field-emission scanning electron microscope (FE-SEM) and high-resolutio
51 try, cyclic voltammetry (CV), field emission scanning electron microscope (FE-SEM) imaging and energy
52 nt analytical techniques like field emission scanning electron microscope (FE-SEM) with an energy dis
53 d by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission
54 erial was characterized using field emission scanning electron microscope (FE-SEM, SEM-Mapping), scan
56 tural characterizations using Field Emission Scanning Electron Microscope (FESEM) and XRD confirmed t
58 n film is characterized using field emission scanning electron microscope (FESEM), energy dispersive
59 C-1-NH(2)-FA were approved by field emission scanning electron microscope (FESEM), transmission elect
60 mposite were characterized by Field Emission Scanning Electron Microscope (FESEM), X-ray diffraction
62 cope (iFLM) inside of a focused ion beam and scanning electron microscope (FIB-SEM) to identify fluor
63 M workflow based on a novel focused ion beam/scanning electron microscope (FIB/SEM) compatible with c
68 Ultraviolet-Vis spectroscopy, field emission scanning electron microscope, high resolution transmissi
70 eural network model, SandAI, that classifies scanning electron microscope images of modern sand grain
76 After the yarn was embedded into knitwear, scanning electron microscope images revealed an intact n
78 rescence confocal, transmission electron and scanning electron microscope images show the preferentia
80 erspectral data sets and the high-resolution scanning electron microscope images were fused into a co
83 hology can be extracted more accurately from scanning electron microscope images, enabling a more inf
84 this technique show excellent agreement with scanning electron microscope images, high spatial resolu
87 arin Red, and Von Kossa staining followed by scanning electron microscope imaging and element mapping
88 ntitative assessments of clot stability, and scanning electron microscope imaging of clot ultrastruct
89 e spectroscopy (EIS) and also field emission scanning electron microscope imaging were used for elect
91 as transferred into a focused ion beam and a scanning electron microscope in which the crystals were
93 a(+) FIB-SEM (Focused Ion Beam combined with Scanning Electron Microscope) instrument is presented.
94 a stylus contact profilometer (n = 4) and a scanning electron microscope (n = 3) at x40 k magnificat
95 scales by optical microscope, environmental scanning electron microscope, nano/microindentation, and
97 visualized using fluorescence microscope and scanning electron microscope, proving the circularity.
99 the L-PRF membranes for 48 hours followed by scanning electron microscope (SEM) analysis immediately
100 mechanical properties were examined using a scanning electron microscope (SEM) and a texture analyze
101 nting poly(AN-co-MSAN) were observed using a scanning electron microscope (SEM) and an atomic force m
102 pectroscopy (FTIR), X-ray diffraction (XRD), Scanning electron microscope (SEM) and Brunauer-Emmett-T
104 orphologies of BNNSs are characterized using scanning electron microscope (SEM) and high-resolution t
107 y of the modified electrode was evaluated by Scanning Electron Microscope (SEM) and Transmission Elec
110 ogical and structural characterizations by a scanning electron microscope (SEM) and X-ray diffraction
112 the materials studied were examined using a scanning electron microscope (SEM) coupled with energy d
116 (LC-mas/mas) to assess the drug release and scanning electron microscope (SEM) for morphological ass
121 proposed for the automatic classification of scanning electron microscope (SEM) images of metal failu
123 tribution of particulates were measured from scanning electron microscope (SEM) images of the collect
124 e MSTN mutant and wild-type (WT) quail eggs, scanning electron microscope (SEM) images was taken.
126 mography (CT), plasma focused ion beam (FIB) scanning electron microscope (SEM) imaging and scanning
128 yzed using atomic force microscope (AFM) and scanning electron microscope (SEM) imaging techniques.
129 ng the secondary electron (SE) signal in the scanning electron microscope (SEM) is a technique gainin
133 rial cryo-focused ion beam (cryoFIB) milling/scanning electron microscope (SEM) volume imaging and la
134 nocomposites properties were accomplished by scanning electron microscope (SEM), electrochemical impe
135 attering (DLS), zeta-potential measurements, scanning electron microscope (SEM), energy-dispersive X-
137 bes in an atomic force microscope (AFM) or a scanning electron microscope (SEM), optical tweezers, an
138 d by X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), quartz crystal micro
140 rier transform infrared (FTIR) spectroscopy, scanning electron microscope (SEM), transmission electro
142 Various characterization methods such as scanning electron microscope (SEM), transmission electro
151 The continuous electron beam of conventional scanning electron microscopes (SEM) limits the temporal
152 d composition distribution were analyzed via scanning electron microscope(SEM) and energy dispersive
153 e surface, while dual focused ion beam (FIB)-scanning electron microscopes (SEMs) operating under cry
154 trast, advances in the spatial resolution of scanning electron microscopes (SEMs), which are by far t
155 situ compression experiments conducted in a scanning electron microscope show an emergent electromec
156 ural surface analysis of the product under a scanning electron microscope showed an increasingly rigi
161 situ fracture-toughness measurements in the scanning electron microscope to characterize effects at
162 ere inspected using a stereomicroscope and a scanning electron microscope to determine the failure mo
163 ackscatter diffraction (EBSD) technique in a scanning electron microscope to non-destructively charac
165 ral circuitry, we generated focused ion beam-scanning electron microscope volumes of the ventral nerv
168 ibution can be observed in the environmental scanning electron microscope, which also reveals the pre
169 by Fourier transform infrared spectroscopy, scanning electron microscope with energy dispersive X-ra
170 nipulation technique inside a field-emission scanning electron microscope with neural network analysi